Evidence map›Paper›PMID 28545845›Full record

ArticleDevelopmental biology2017

Claudins are essential for cell shape changes and convergent extension movements during neural tube closure.

Amanda I Baumholtz, Annie Simard, Evanthia Nikolopoulou, Marcus Oosenbrug, Michelle M Collins, Anna Piontek, Gerd Krause, Jörg Piontek, Nicholas D E Greene, Aimee K Ryan

Open access · hybridAbstract read
In one paragraph

Article in Developmental biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.0field-weighted citation impact, top 23% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

17 citing papers in PubMed, 34 citations in OpenAlex.

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  15. Functional Validation ofFrontiers in neuroscience · 2020
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 5 institutions in 3 countries.

Amanda I BaumholtzDepartment of Human Genetics, McGill University, Canada; The Research Institute of the McGill University Health Centre, Montréal, Québec, Canada. Electronic address: amanda.baumholtz@mail.mcgill.ca.
Annie SimardDepartment of Experimental Medicine, McGill University, Canada; The Research Institute of the McGill University Health Centre, Montréal, Québec, Canada. Electronic address: annie.simard2@mail.mcgill.ca.
Evanthia NikolopoulouDevelopmental Biology and Cancer Programme, Birth Defects Research Centre, UCL Institute of Child Health, London, UK. Electronic address: e.nikolopoulou@ucl.ac.uk.
Marcus OosenbrugDepartment of Anatomy and Cell Biology, McGill University, Canada; The Research Institute of the McGill University Health Centre, Montréal, Québec, Canada. Electronic address: marcus.oosenbrug@mail.mcgill.ca.
Michelle M CollinsDepartment of Human Genetics, McGill University, Canada; The Research Institute of the McGill University Health Centre, Montréal, Québec, Canada. Electronic address: michelle.collins@mpi-bn.mpg.de.
Anna PiontekLeibniz-Forschungsinstitut für Molekulare Pharmakologie, FMP, Berlin, Germany. Electronic address: apiontek@fmp-berlin.de.
Gerd KrauseLeibniz-Forschungsinstitut für Molekulare Pharmakologie, FMP, Berlin, Germany. Electronic address: gkrause@fmp-berlin.de.
Jörg PiontekInstitute of Clinical Physiology, Charité-Universitätsmedizin Berlin, Berlin, Germany. Electronic address: joerg.piontek@charite.de.
Nicholas D E GreeneDevelopmental Biology and Cancer Programme, Birth Defects Research Centre, UCL Institute of Child Health, London, UK. Electronic address: n.greene@ucl.ac.uk.
Aimee K RyanDepartment of Human Genetics, McGill University, Canada; Department of Experimental Medicine, McGill University, Canada; Department of Pediatrics, McGill University, Canada; The Research Institute of the McGill University Health Centre, Montréal, Québec, Canada. Electronic address: aimee.ryan@mcgill.ca.
McGill University Health Centre · CALeibniz-Forschungsinstitut für Molekulare Pharmakologie · DEMcGill University · CAUniversity College London · GBCharité - Universitätsmedizin Berlin · DE

Funding

CIHR MOP-84583Medical Research Council G0802163
6 · The paper itself

Abstract

During neural tube closure, regulated changes at the level of individual cells are translated into large-scale morphogenetic movements to facilitate conversion of the flat neural plate into a closed tube. Throughout this process, the integrity of the neural epithelium is maintained via cell interactions through intercellular junctions, including apical tight junctions. Members of the claudin family of tight junction proteins regulate paracellular permeability, apical-basal cell polarity and link the tight junction to the actin cytoskeleton. Here, we show that claudins are essential for neural tube closure: the simultaneous removal of Cldn3, -4 and -8 from tight junctions caused folate-resistant open neural tube defects. Their removal did not affect cell type differentiation, neural ectoderm patterning nor overall apical-basal polarity. However, apical accumulation of Vangl2, RhoA, and pMLC were reduced, and Par3 and Cdc42 were mislocalized at the apical cell surface. Our data showed that claudins act upstream of planar cell polarity and RhoA/ROCK signaling to regulate cell intercalation and actin-myosin contraction, which are required for convergent extension and apical constriction during neural tube closure, respectively.

Indexed as

Actin CytoskeletonAdaptor Proteins, Signal TransducingAnimalscdc42 GTP-Binding ProteinCell Adhesion MoleculesCell Cycle ProteinsCell PolarityCell ShapeChick EmbryoClaudin-3Claudin-4ClaudinsEmbryo Culture TechniquesMiceMorphogenesisNerve Tissue ProteinsAdaptor Proteins, Signal Transducingcdc42 GTP-Binding ProteinCdc42 protein, mouseCell Adhesion MoleculesCell Cycle ProteinsClaudin-3Claudin-4claudin 8ClaudinsCldn3 protein, mouseCldn4 protein, mouseLtap protein, mouseNerve Tissue ProteinsPard3 protein, mouserhoA GTP-Binding ProteinRhoA protein, mouserho GTP-Binding ProteinsApical constrictionClaudinConvergent extensionNeural tube defectsTight junctions

Identifiers

PMID28545845
PMCPMC5523803
OpenAlexW2617546415

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.